Structure of PDB 7jvk Chain B Binding Site BS01
Receptor Information
>7jvk Chain B (length=448) Species:
330879
(Aspergillus fumigatus Af293) [
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LRSTPQDELHDLLCVGFGPASLAIAIALHDALDPRLNKSASNIHAQPKIC
FLERQKQFAWHSGMLVPGSKAQISFIKDLATLRDPRSSFTFLNYLHQKGR
LIHFTNLSTFLPARLEFEDYMRWCAQQFSDVVAYGEEVVEVIPGKSDPSS
SVVDFFTVRSRNVETGEISARRTRKVVIAIGGTAKMPSGLPQDPRIIHSS
KYCTTLPALLKDKSKPYNIAVLGSGQSAAEIFHDLQKRYPNSRTTLIMRD
SAMRPSDDSPFVNEIFNPERVDKFYSQSAAERQRSLLADKATNYSVVRLE
LIEEIYNDMYLQRVKNPDETQWQHRILPERKITRVEHHGPQSRMRIHLKS
SKETLEVDALMVATGYNRNAHERLLSKVQHLRPTGQDQWKPHRDYRVEMD
PSKVSSEAGIWLQGCNERTHGLSDSLLSVLAVRGGEMVQSIFGEQLER
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
7jvk Chain B Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
7jvk
Structural Determinants of Flavin Dynamics in a Class B Monooxygenase.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
G46 G48 P49 A50 E83 R84 Q85 W90 H91 E167 V168 I210 G211 N323 Y324 S466
Binding residue
(residue number reindexed from 1)
G16 G18 P19 A20 E53 R54 Q55 W60 H61 E137 V138 I180 G181 N293 Y294 S425
Annotation score
2
Enzymatic activity
Enzyme Commision number
1.14.13.196
: L-ornithine N(5)-monooxygenase [NAD(P)H].
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004497
monooxygenase activity
GO:0004499
N,N-dimethylaniline monooxygenase activity
GO:0005506
iron ion binding
GO:0031172
ornithine N5-monooxygenase activity
GO:0070401
NADP+ binding
Biological Process
GO:0006696
ergosterol biosynthetic process
GO:0006879
intracellular iron ion homeostasis
GO:0009058
biosynthetic process
GO:0010106
cellular response to iron ion starvation
GO:0019290
siderophore biosynthetic process
GO:0031169
ferrichrome biosynthetic process
GO:0033214
siderophore-dependent iron import into cell
GO:0044550
secondary metabolite biosynthetic process
Cellular Component
GO:0005575
cellular_component
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Molecular Function
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Cellular Component
External links
PDB
RCSB:7jvk
,
PDBe:7jvk
,
PDBj:7jvk
PDBsum
7jvk
PubMed
33226785
UniProt
E9QYP0
|SIDA_ASPFU L-ornithine N(5)-monooxygenase (Gene Name=sidA)
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